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Review of Pharmacology - 9E (2015)

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Cardiovascular System<br />

43. Ans. (d) Hypertrophic obstructive cardiomyopathy (Ref: KDT 6/e p500-502)<br />

44. Ans. (a) Lisinopril (Ref: KDT 6/e p486)<br />

45. Ans. (a) Adrenaline (Ref: KDT 6/e p493,503-504)<br />

46. Ans. (d) Hyperkalemia (Ref: KDT 6/e p499)<br />

47. Ans. (b) 0.8-1.5 ng/ml (Ref: KDT 6/e p497)<br />

Digitoxin<br />

Digoxin<br />

– Therapeutic plasma conc. 15-30 ng/ml 0.5-1.4 ng/ml<br />

– Toxic plasma conc. > 35 ng/ml > 2.5 ng/ml<br />

48. Ans. (c) Treat digitalis toxicity (Ref: KDT 6/e p499)<br />

49. Ans. (c) It is 95% plasma protein bound (Ref: KDT 6/e p497)<br />

Plasma protein binding <strong>of</strong> digitoxin is high (95%) whereas it is low (70-80%) for digoxin.<br />

50. Ans. (b) Propanolol (Ref: KDT 6/e p504)<br />

Afterload is reduced by the drugs having arteriolar dilating property. Propanolol is a non-selective b-blocker. It can cause<br />

vasoconstriction by antagonizing b 2<br />

mediated vasodilatation. It, therefore do not decrease afterload.<br />

51. Ans. (a) Guanylate cyclase (Ref: KDT 6/e p548-549)<br />

Nitroprusside generates NO that relaxes vascular smooth muscles by activating guanylate cyclase.<br />

52. Ans. (d) Na + K + ATPase (Ref: KDT 6/e p496)<br />

53. Ans. (c) 5 day (Ref: KDT 6/e p497)<br />

54. Ans. (a) Hydralazine (Ref: KDT 6/e p547)<br />

55. Ans. (d) All <strong>of</strong> the above (Ref: KDT 6/e p498)<br />

56. Ans. (b) Morphine (Ref: KDT 6/e p461)<br />

57. Ans. (a) Na + K + ATPase pump (Ref: KDT 6/e p496)<br />

58. Ans. (b) Captopril (Ref: Katzung 11/e p219)<br />

59. Ans. (c) An increase in systolic intracellular calcium levels (Ref: Katzung 11/e p214)<br />

60. Ans. (d) Fab fragments <strong>of</strong> digitalis antibodies (Ref: KDT 6/e p499)<br />

61. Ans. (c) NPAT with block (Ref: KDT 6/e p498)<br />

62. Ans. (c) Sodium nitroprusside (Ref: KDT 7/e p567-568)<br />

Increase in systemic vascular resistance means vasoconstriction, thus a vasodilator drug like nitroprusside should be used.<br />

Adrenaline and nor-adrenaline act as vasopressors whereas isoprenaline increases systolic blood pressure by acting on<br />

heart.<br />

63. Ans. (a) Propanolol (Ref: Katzung 10/e p165, 169; KDT 6/e p137)<br />

• Methyldopa is useful in the treatment <strong>of</strong> mild to moderately severe hypertension. It lowers blood pressure chiefly by<br />

reducing peripheral vascular resistance, with a variable reduction in heart rate and cardiac output.<br />

• Prazosin and nitroprusside are vasodilators and produce reflex tachycardia instead <strong>of</strong> causing bradycardia.<br />

• Propanolol is a non selective beta blocker and acts mainly by decreasing heart rate.<br />

64. Ans. (a) Atenolol (Ref: KDT 6/e p139), Current hypertensive research May 2012; Antihypertensive treatment and sexual dysfunction.<br />

• Diuretics have maximum risk <strong>of</strong> causing sexual dysfunction followed by beta blockers.<br />

• Atenolol, metoprolol and carvedilol have high risk whereas nevibolol has minimum risk <strong>of</strong> erectile dysfunction.<br />

• ACE inhibitors decrease the risk.<br />

65. Ans. (b) It can cause severe hypoglycemia (Ref: Katzung 11/e p180)<br />

Diazoxide cause hyperglycemia and not hypoglycemia<br />

General Cardiovascular <strong>Pharmacology</strong> System<br />

• Diazoxide is an effective and relatively long-acting parenterally administered arteriolar dilator that is occasionally<br />

used to treat hypertensive emergencies.<br />

• It acts by opening ATP sensitive potassium channels.<br />

• The most significant toxicity from diazoxide has been excessive hypotension.<br />

• Diazoxide inhibits insulin release from the pancreas (probably by opening potassium channels in the cell<br />

membrane) and is used to treat hypoglycemia secondary to insulinoma.<br />

• Occasionally, hyperglycemia complicates diazoxide use, particularly in persons with renal insufficiency.<br />

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